ATE533770T1 - PYRAZOLOPYRIMIDINES AS PROTEIN KINASE INHIBITORS - Google Patents
PYRAZOLOPYRIMIDINES AS PROTEIN KINASE INHIBITORSInfo
- Publication number
- ATE533770T1 ATE533770T1 AT06816408T AT06816408T ATE533770T1 AT E533770 T1 ATE533770 T1 AT E533770T1 AT 06816408 T AT06816408 T AT 06816408T AT 06816408 T AT06816408 T AT 06816408T AT E533770 T1 ATE533770 T1 AT E533770T1
- Authority
- AT
- Austria
- Prior art keywords
- pyrazolopyrimidines
- protein kinase
- kinase inhibitors
- inhibitors
- protein
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US72419705P | 2005-10-06 | 2005-10-06 | |
PCT/US2006/039136 WO2007041712A1 (en) | 2005-10-06 | 2006-10-04 | Pyrazolopyrimidines as protein kinase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE533770T1 true ATE533770T1 (en) | 2011-12-15 |
Family
ID=37560916
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT06816408T ATE533770T1 (en) | 2005-10-06 | 2006-10-04 | PYRAZOLOPYRIMIDINES AS PROTEIN KINASE INHIBITORS |
Country Status (18)
Country | Link |
---|---|
US (1) | US7776865B2 (en) |
EP (1) | EP1931676B1 (en) |
JP (2) | JP5052518B2 (en) |
KR (1) | KR20080063806A (en) |
CN (1) | CN101321760A (en) |
AR (1) | AR056206A1 (en) |
AT (1) | ATE533770T1 (en) |
AU (1) | AU2006299338A1 (en) |
BR (1) | BRPI0617150A2 (en) |
CA (1) | CA2624882C (en) |
EC (1) | ECSP088350A (en) |
IL (1) | IL190598A0 (en) |
NO (1) | NO20082092L (en) |
PE (1) | PE20070543A1 (en) |
RU (1) | RU2008117298A (en) |
TW (1) | TW200745123A (en) |
WO (1) | WO2007041712A1 (en) |
ZA (1) | ZA200802995B (en) |
Families Citing this family (65)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1931676B1 (en) * | 2005-10-06 | 2011-11-16 | Schering Corporation | Pyrazolopyrimidines as protein kinase inhibitors |
WO2007044441A2 (en) * | 2005-10-06 | 2007-04-19 | Schering Corporation | Use of pyrazolo [1 , 5 -a] pyrimidine derivatives for inhibiting protein kinases methods for inhibiting protein kinases |
MX2008011430A (en) * | 2006-03-08 | 2008-09-18 | Novartis Ag | Use of pyrazolo[1,5a]pyrimidin-7-yl amine derivatives in the treatment of neurological disorders. |
EP2027127A1 (en) * | 2006-05-22 | 2009-02-25 | Shering Corporation | Pyrazolo [1, 5-a]pyrimidines as cdk inhibitors |
ES2403546T3 (en) | 2006-11-03 | 2013-05-20 | Pharmacyclics, Inc. | Bruton tyrosine kinase activity probe and method of use |
KR101546493B1 (en) * | 2006-11-06 | 2015-08-21 | 톨레로 파마수티컬스, 인크. | [12-] [15-] Imidazo[12-B]pyridazine and pyrazolo[15-A]pyrimidine derivatives and their use as protein kinase inhibitors |
TW200845962A (en) | 2007-05-08 | 2008-12-01 | Schering Corp | Methods of treatment using intravenous formulations comprising temozolomide |
US8124759B2 (en) | 2007-05-09 | 2012-02-28 | Abbott Laboratories | Inhibitors of protein kinases |
ES2372559T3 (en) * | 2007-05-09 | 2012-01-23 | Abbott Laboratories | HETEROCYCLIC COMPOUNDS CONDENSED AS PROTEIN QUINASE INHIBITORS. |
WO2008141140A1 (en) * | 2007-05-09 | 2008-11-20 | Abbott Laboratories | Condensed heterocyclic compounds as inhibitors of protein kinases |
WO2009004329A1 (en) * | 2007-07-02 | 2009-01-08 | Cancer Research Technology Limited | 9h-pyrimido[4,5-b]indoles, 9h-pyrido[4',3':4,5]pyrrolo[2,3-d]pyridines, and 9h-1,3,6,9-tetraaza-fluorenes as chk1 kinase function inhibitors |
CA2705092A1 (en) * | 2007-11-07 | 2009-05-14 | Schering Corporation | Novel modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors |
US8426441B2 (en) * | 2007-12-14 | 2013-04-23 | Roche Palo Alto Llc | Inhibitors of bruton's tyrosine kinase |
WO2009077334A1 (en) | 2007-12-14 | 2009-06-25 | F. Hoffmann-La Roche Ag | Novel imidazo[1,2-a]pyridine and imidazo[1,2-b]pyridazine derivatives |
EP2265603B1 (en) | 2008-03-13 | 2014-05-07 | The General Hospital Corporation | Inhibitors of the bmp signaling pathway |
JP2011519973A (en) * | 2008-05-12 | 2011-07-14 | アムネスティックス・インコーポレーテッド | Information about compound-related applications to improve learning and memory |
CL2009001152A1 (en) | 2008-05-13 | 2009-10-16 | Array Biopharma Inc | Compounds derived from n- (4- (nitrogen cycloalkyl-1-yl) -1h-pyrrolo [2,3-b] pyridin-3-yl) amide, kinase inhibitors; Preparation process; pharmaceutical composition; and its use for the treatment of a proliferative disease. |
PA8851101A1 (en) * | 2008-12-16 | 2010-07-27 | Lilly Co Eli | AMINO PIRAZOL COMPOUND |
US8957064B2 (en) * | 2009-02-13 | 2015-02-17 | Bayer Intellectual Property Gmbh | Fused pyrimidines |
EP2413932A4 (en) * | 2009-04-01 | 2012-09-19 | Merck Sharp & Dohme | Inhibitors of akt activity |
UA110324C2 (en) * | 2009-07-02 | 2015-12-25 | Genentech Inc | Jak inhibitory compounds based on pyrazolo pyrimidine |
US8993535B2 (en) | 2009-09-04 | 2015-03-31 | Merck Sharp & Dohme Corp. | Modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors |
AR079234A1 (en) * | 2009-12-01 | 2012-01-04 | Abbott Lab | NITROGEN CONDENSED HETEROCICLIC DERIVATIVES, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND USE OF THE SAME TO TREAT ONCOLOGICAL AFFECTIONS, THE NERVOUS SYSTEM AND / OR THE IMMUNE SYSTEM. |
WO2012007416A1 (en) * | 2010-07-13 | 2012-01-19 | Bayer Pharma Aktiengesellschaft | Bicyclic pyrimidines |
WO2012013713A2 (en) * | 2010-07-28 | 2012-02-02 | Bayer Pharma Aktiengesellschaft | Substituted imidazo[1,2-b]pyridazines |
WO2012178125A1 (en) | 2011-06-22 | 2012-12-27 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
ES2834093T3 (en) | 2011-07-21 | 2021-06-16 | Sumitomo Dainippon Pharma Oncology Inc | Heterocyclic protein kinase inhibitors |
CA2849566C (en) | 2011-11-09 | 2021-02-09 | Cancer Research Technology Limited | 5-(pyridin-2-yl-amino)-pyrazine-2-carbonitrile compounds and their therapeutic use |
ES2589955T3 (en) * | 2012-01-10 | 2016-11-17 | Bayer Intellectual Property Gmbh | Substituted pyrazolopyrimidines as Akt kinase inhibitors |
EP2855448B1 (en) | 2012-05-15 | 2017-02-08 | Cancer Research Technology Ltd | 5-[[4-[[morpholin-2-yl]methylamino]-5-(trifluoromethyl)-2-pyridyl]amino]pyrazine-2-carbonitrile and therapeutic uses thereof |
PL3808749T3 (en) | 2012-12-07 | 2023-07-10 | Vertex Pharmaceuticals Incorporated | Pyrazolo[1,5-a]pyrimidines useful as inhibitors of atr kinase for the treatment of cancer diseases |
WO2014110574A1 (en) | 2013-01-14 | 2014-07-17 | Incyte Corporation | Bicyclic aromatic carboxamide compounds useful as pim kinase inhibitors |
SG10201705662WA (en) | 2013-01-15 | 2017-08-30 | Incyte Corp | Thiazolecarboxamides and pyridinecarboxamide compounds useful as pim kinase inhibitors |
WO2014160203A2 (en) | 2013-03-14 | 2014-10-02 | The Brigham And Women's Hospital, Inc. | Bmp inhibitors and methods of use thereof |
WO2014143240A1 (en) | 2013-03-15 | 2014-09-18 | Vertex Pharmaceuticals Incorporated | Fused pyrazolopyrimidine derivatives useful as inhibitors of atr kinase |
EP2970288A1 (en) | 2013-03-15 | 2016-01-20 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
EP2970289A1 (en) | 2013-03-15 | 2016-01-20 | Vertex Pharmaceuticals Inc. | Compounds useful as inhibitors of atr kinase |
PL3023100T3 (en) | 2013-07-18 | 2019-07-31 | Taiho Pharmaceutical Co., Ltd. | Antitumor drug for intermittent administration of fgfr inhibitor |
US10124003B2 (en) | 2013-07-18 | 2018-11-13 | Taiho Pharmaceutical Co., Ltd. | Therapeutic agent for FGFR inhibitor-resistant cancer |
PE20160532A1 (en) | 2013-08-23 | 2016-05-21 | Incyte Corp | COMPOUND OF FURO CARBOXAMIDE AND TENOPYRIDINE USEFUL AS INHIBITORS OF PIM KINASES |
JP6543252B2 (en) | 2013-12-06 | 2019-07-10 | バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated | 2-Amino-6-fluoro-N- [5-fluoro-pyridin-3-yl] pyrazolo [1,5-a] pyrimidine-3-carboxamide compounds useful as ATR kinase inhibitors, their preparation, their different solid forms And radiolabeled derivatives |
MX2016015874A (en) | 2014-06-05 | 2017-03-27 | Vertex Pharma | Radiolabelled derivatives of a 2-amino-6-fluoro-n-[5-fluoro-pyrid in-3-yl]- pyrazolo[1,5-a]pyrimidin-3-carboxamide compound useful as atr kinase inhibitor, the preparation of said compound and different solid forms thereof. |
PT3157566T (en) | 2014-06-17 | 2019-07-11 | Vertex Pharma | Method for treating cancer using a combination of chk1 and atr inhibitors |
US9580418B2 (en) | 2014-07-14 | 2017-02-28 | Incyte Corporation | Bicyclic aromatic carboxamide compounds useful as Pim kinase inhibitors |
WO2016010897A1 (en) | 2014-07-14 | 2016-01-21 | Incyte Corporation | Bicyclic heteroaromatic carboxamide compounds useful as pim kinase inhibitors |
WO2016011019A1 (en) | 2014-07-15 | 2016-01-21 | The Brigham And Women's Hospital, Inc. | Compositions and methods for inhibiting bmp |
TW201702218A (en) | 2014-12-12 | 2017-01-16 | 美國杰克森實驗室 | Compositions and methods relating to the treatment of cancer, autoimmune disease, and neurodegenerative disease |
AU2016240841C1 (en) | 2015-03-31 | 2018-05-17 | Taiho Pharmaceutical Co., Ltd. | Crystal of 3,5-disubstituted benzene alkynyl compound |
WO2016196244A1 (en) | 2015-05-29 | 2016-12-08 | Incyte Corporation | Pyridineamine compounds useful as pim kinase inhibitors |
TWI734699B (en) | 2015-09-09 | 2021-08-01 | 美商英塞特公司 | Salts of a pim kinase inhibitor |
CA3000684A1 (en) | 2015-09-30 | 2017-04-06 | Vertex Pharmaceuticals Incorporated | Method for treating cancer using a combination of dna damaging agents and atr inhibitors |
TW201718546A (en) | 2015-10-02 | 2017-06-01 | 英塞特公司 | Heterocyclic compounds useful as PIM kinase inhibitors |
US11883404B2 (en) | 2016-03-04 | 2024-01-30 | Taiho Pharmaceuticals Co., Ltd. | Preparation and composition for treatment of malignant tumors |
KR20240014585A (en) | 2016-03-04 | 2024-02-01 | 다이호야쿠힌고교 가부시키가이샤 | Preparation and composition for treatment of malignant tumors |
TW201902896A (en) * | 2017-05-22 | 2019-01-16 | 瑞士商赫孚孟拉羅股份公司 | Therapeutic compounds and compositions and methods of use thereof |
JP7216705B2 (en) * | 2017-07-28 | 2023-02-02 | ニンバス ラクシュミ, インコーポレイテッド | TYK2 inhibitors and methods of use thereof |
US10596161B2 (en) | 2017-12-08 | 2020-03-24 | Incyte Corporation | Low dose combination therapy for treatment of myeloproliferative neoplasms |
US11833151B2 (en) | 2018-03-19 | 2023-12-05 | Taiho Pharmaceutical Co., Ltd. | Pharmaceutical composition including sodium alkyl sulfate |
CN117838695A (en) | 2018-04-13 | 2024-04-09 | 住友制药肿瘤公司 | PIM kinase inhibitors for the treatment of myeloproliferative neoplasms and cancer-related fibrosis |
CN108586341B (en) * | 2018-05-25 | 2020-05-08 | 天津商业大学 | Amide compounds and medicinal salts thereof, and preparation method and medicinal application thereof |
AU2019360941A1 (en) * | 2018-10-15 | 2021-04-29 | Takeda Pharmaceutical Company Limited | TYK2 inhibitors and uses thereof |
CN109293630A (en) * | 2018-11-15 | 2019-02-01 | 山东大学 | Compound of class containing substituted pyrazolecarboxylic and the preparation method and application thereof |
CN113412262A (en) | 2019-02-12 | 2021-09-17 | 大日本住友制药肿瘤公司 | Formulations comprising heterocyclic protein kinase inhibitors |
CN112457306A (en) * | 2019-09-06 | 2021-03-09 | 上海瑛派药业有限公司 | 3, 5-disubstituted pyrazole compounds as kinase inhibitors and application thereof |
CN114957261B (en) * | 2022-05-17 | 2023-06-23 | 重庆文理学院 | Compound with anti-head and neck cancer effect and preparation method and application thereof |
Family Cites Families (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3130633A1 (en) * | 1981-08-01 | 1983-02-17 | Basf Ag, 6700 Ludwigshafen | 7-AMINO-AZOLO (1,5-A) PYRIMIDINE AND FUNGICIDES CONTAINING THEM |
KR100191774B1 (en) | 1991-04-22 | 1999-06-15 | 오스카 아끼히꼬 | Pyrazolo(1,5-alpha)pyrimidine derivatives and anti-inflammatory agent containing them |
EP0628559B1 (en) | 1993-06-10 | 2002-04-03 | Beiersdorf-Lilly GmbH | Pyrimidine compounds and their use as pharmaceuticals |
US5571813A (en) | 1993-06-10 | 1996-11-05 | Beiersdorf-Lilly Gmbh | Fused pyrimidine compounds and their use as pharmaceuticals |
CN1046730C (en) | 1994-06-21 | 1999-11-24 | 株式会社大塚制药工场 | Pyrazolo [1,5-a] pyrimidine derivative |
US6313124B1 (en) | 1997-07-23 | 2001-11-06 | Dupont Pharmaceuticals Company | Tetrazine bicyclic compounds |
JP2002501532A (en) | 1997-05-30 | 2002-01-15 | メルク エンド カンパニー インコーポレーテッド | Novel angiogenesis inhibitors |
ATE355841T1 (en) | 1997-12-13 | 2007-03-15 | Bristol Myers Squibb Co | USE OF PYRAZOLO (3,4-B)PYRIDINE AS A CYCLINE-DEPENDENT KINASE INHIBITOR |
US6413974B1 (en) | 1998-02-26 | 2002-07-02 | Aventis Pharmaceuticals Inc. | 6,9,-disubstituted 2-[trans-(4-aminocyclohexyl) amino] purines |
JP4876239B2 (en) | 1999-01-11 | 2012-02-15 | プリンストン ユニバーシティー | High affinity inhibitors for target confirmation and use thereof |
FR2805160B1 (en) * | 2000-02-23 | 2002-04-05 | Oreal | COMPOSITIONS FOR OXIDATION DYEING OF KERATINIC FIBERS COMPRISING N (2-HYDROXYBENZENE) -CARBRAMATE OR N- (2-HYDROXYBENZENE) -UREA AND PYRAZOLOPYRIMIDINE, AND DYEING METHODS |
CN100457753C (en) | 2000-07-26 | 2009-02-04 | 布里斯托尔-迈尔斯斯奎布公司 | N-[5-[[[5-alkyl-2-oxazolyl]methyl]thio]-2-thiazolyl] carboxamide inhibitors of cyclin dependent kinases |
ZA200301696B (en) | 2000-09-15 | 2004-04-28 | Vertex Pharma | Isoxazoles and their use as inhibitors of erk. |
US7067520B2 (en) | 2000-11-17 | 2006-06-27 | Ishihara Sangyo Kaisha, Ltd. | Preventive or therapeutic medicines for diabetes containing fused-heterocyclic compounds or their salts |
JP2002212076A (en) * | 2000-11-17 | 2002-07-31 | Ishihara Sangyo Kaisha Ltd | Prophylactic or therapeutic agent for diabetes comprising condensed heterocyclic compound or its salt |
AU2509602A (en) | 2000-12-20 | 2002-07-01 | Sod Conseils Rech Applic | Cyclin-dependent kinase (CDK) and glycolene synthase kinase-3 (GSK-3) inhibitors |
CA2483306A1 (en) | 2002-04-23 | 2003-11-06 | Shionogi & Co., Ltd. | Pyrazolo[1,5-a]pyrimidine derivative and nad(p)h oxidase inhibitor containing the same |
DE10223917A1 (en) | 2002-05-29 | 2003-12-11 | Bayer Cropscience Ag | New 7-amino-6-aryl-pyrazolo-(1,5-a)-pyrimidine derivatives, useful as pesticides, e.g. insecticides, acaricides, nematocides, bactericides or especially fungicides for protection of plants or materials |
WO2003101993A1 (en) | 2002-06-04 | 2003-12-11 | Neogenesis Pharmaceuticals, Inc. | Pyrazolo` 1,5a! pyrimidine compounds as antiviral agents |
KR101088922B1 (en) * | 2002-09-04 | 2011-12-01 | 파마코페이아, 엘엘씨. | Pyrazolopyrimidines as cyclin-dependent kinase inhibitors |
WO2004089416A2 (en) | 2003-04-11 | 2004-10-21 | Novo Nordisk A/S | Combination of an 11beta-hydroxysteroid dehydrogenase type 1 inhibitor and an antihypertensive agent |
PE20051089A1 (en) | 2004-01-22 | 2006-01-25 | Novartis Ag | PYRAZOLE [1,5-A] PYRIMIDIN-7-IL-AMINE DERIVATIVES AS PROTEIN KINASE INHIBITORS |
ATE448229T1 (en) * | 2005-01-19 | 2009-11-15 | Merck & Co Inc | BICYCLIC PYRIMIDINES AS DIPEPTIDYLPEPTIDASE IV INHIBITORS FOR THE TREATMENT OR PREVENTION OF DIABETES |
GB0515026D0 (en) * | 2005-07-21 | 2005-08-31 | Novartis Ag | Organic compounds |
EP1931676B1 (en) * | 2005-10-06 | 2011-11-16 | Schering Corporation | Pyrazolopyrimidines as protein kinase inhibitors |
-
2006
- 2006-10-04 EP EP06816408A patent/EP1931676B1/en active Active
- 2006-10-04 WO PCT/US2006/039136 patent/WO2007041712A1/en active Application Filing
- 2006-10-04 PE PE2006001206A patent/PE20070543A1/en not_active Application Discontinuation
- 2006-10-04 RU RU2008117298/04A patent/RU2008117298A/en not_active Application Discontinuation
- 2006-10-04 CN CNA2006800455049A patent/CN101321760A/en active Pending
- 2006-10-04 CA CA2624882A patent/CA2624882C/en not_active Expired - Fee Related
- 2006-10-04 BR BRPI0617150-8A patent/BRPI0617150A2/en not_active IP Right Cessation
- 2006-10-04 TW TW095136815A patent/TW200745123A/en unknown
- 2006-10-04 AR ARP060104364A patent/AR056206A1/en not_active Application Discontinuation
- 2006-10-04 US US11/542,921 patent/US7776865B2/en active Active
- 2006-10-04 JP JP2008534711A patent/JP5052518B2/en not_active Expired - Fee Related
- 2006-10-04 AU AU2006299338A patent/AU2006299338A1/en not_active Abandoned
- 2006-10-04 KR KR1020087010465A patent/KR20080063806A/en not_active Application Discontinuation
- 2006-10-04 AT AT06816408T patent/ATE533770T1/en active
-
2008
- 2008-04-03 IL IL190598A patent/IL190598A0/en unknown
- 2008-04-04 EC EC2008008350A patent/ECSP088350A/en unknown
- 2008-04-04 ZA ZA200802995A patent/ZA200802995B/en unknown
- 2008-05-05 NO NO20082092A patent/NO20082092L/en not_active Application Discontinuation
-
2012
- 2012-01-27 JP JP2012015794A patent/JP2012082233A/en not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
ECSP088350A (en) | 2008-05-30 |
NO20082092L (en) | 2008-07-04 |
JP2012082233A (en) | 2012-04-26 |
CN101321760A (en) | 2008-12-10 |
JP2009511491A (en) | 2009-03-19 |
JP5052518B2 (en) | 2012-10-17 |
BRPI0617150A2 (en) | 2011-07-12 |
EP1931676B1 (en) | 2011-11-16 |
PE20070543A1 (en) | 2007-06-14 |
US7776865B2 (en) | 2010-08-17 |
TW200745123A (en) | 2007-12-16 |
WO2007041712A1 (en) | 2007-04-12 |
RU2008117298A (en) | 2009-11-20 |
AR056206A1 (en) | 2007-09-26 |
US20070083044A1 (en) | 2007-04-12 |
CA2624882A1 (en) | 2007-04-12 |
ZA200802995B (en) | 2009-02-25 |
IL190598A0 (en) | 2008-11-03 |
KR20080063806A (en) | 2008-07-07 |
EP1931676A1 (en) | 2008-06-18 |
AU2006299338A1 (en) | 2007-04-12 |
CA2624882C (en) | 2014-05-20 |
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